Hyperstable in-frame insertion variant of antithrombin. Determined by X-ray diffraction at 2.8 Å resolution. Released 18 Jul 2012.
Explore 4EB1 in 3D Show helices and sheets RCSB PDB PDBe
4EB1 contains 33 α-helices and 42 β-strands across 2 chains. Residue ranges use author residue numbering, as in the PDB file, from PDBe. To see them in 3D, choose the Cartoon representation with Secondary structure coloring: helices, sheets and coils get different colors.
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 24 | 1 | 1 |
| α-helix | 25-26 | 2 | |
| α-helix | 46-68 | 23 | |
| β-strand | 76-78 | 3 | 2 |
| α-helix | 80-90 | 11 | |
| α-helix | 91-93 | 3 | |
| α-helix | 96-105 | 10 | |
| α-helix | 108-110 | 3 | |
| β-strand | 115 | 1 | 1 |
| α-helix | 116-127 | 12 | |
| α-helix | 128-132 | 5 | |
| β-strand | 138-149 | 12 | 3 |
| β-strand | 154 | 1 | 4 |
| α-helix | 156-166 | 11 | |
| β-strand | 169-173 | 5 | 3 |
| α-helix | 179-193 | 15 | |
| β-strand | 204-214 | 11 | 3 |
| β-strand | 219-232 | 14 | 3 |
| β-strand | 233 | 1 | 5 |
| α-helix | 236-238 | 3 | |
| α-helix | 239-241 | 3 | |
| β-strand | 243-248 | 6 | 2 |
| β-strand | 254-270 | 17 | 2 |
| α-helix | 272-274 | 3 | |
| β-strand | 276-281 | 6 | 2 |
| β-strand | 282 | 1 | 5 |
| β-strand | 287-293 | 7 | 2 |
| α-helix | 300-306 | 7 | |
| α-helix | 309-317 | 9 | |
| β-strand | 320-329 | 10 | 2 |
| β-strand | 332-338 | 7 | 3 |
| α-helix | 340-345 | 6 | |
| α-helix | 350-352 | 3 | |
| α-helix | 360-362 | 3 | |
| β-strand | 363 | 1 | 4 |
| β-strand | 370-382 | 13 | 3 |
| β-strand | 384 | 1 | 3 |
| β-strand | 387-388 | 2 | 3 |
| β-strand | 396-398 | 3 | 6 |
| β-strand | 408-411 | 4 | 2 |
| β-strand | 416-422 | 7 | 2 |
| β-strand | 427-434 | 8 | 2 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 45-68 | 24 | |
| β-strand | 76-78 | 3 | 6 |
| α-helix | 80-91 | 12 | |
| α-helix | 96-105 | 10 | |
| α-helix | 108-110 | 3 | |
| α-helix | 116-118 | 3 | |
| α-helix | 119-131 | 13 | |
| β-strand | 139-149 | 11 | 7 |
| β-strand | 154 | 1 | 8 |
| α-helix | 156-165 | 10 | |
| β-strand | 169-173 | 5 | 7 |
| α-helix | 179-193 | 15 | |
| β-strand | 213-224 | 12 | 7 |
| β-strand | 225 | 1 | 9 |
| α-helix | 228-230 | 3 | |
| α-helix | 231-233 | 3 | |
| β-strand | 235-240 | 6 | 6 |
| β-strand | 246-262 | 17 | 6 |
| α-helix | 264-266 | 3 | |
| β-strand | 268-273 | 6 | 6 |
| β-strand | 274 | 1 | 9 |
| β-strand | 279-285 | 7 | 6 |
| α-helix | 292-296 | 5 | |
| α-helix | 301-310 | 10 | |
| β-strand | 312-322 | 11 | 6 |
| β-strand | 323-330 | 8 | 7 |
| α-helix | 332-337 | 6 | |
| α-helix | 342-344 | 3 | |
| β-strand | 355 | 1 | 8 |
| β-strand | 364-375 | 12 | 7 |
| β-strand | 379-390 | 12 | 7 |
| β-strand | 408-414 | 7 | 6 |
| β-strand | 419-426 | 8 | 6 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Antithrombin-III | I | protein | 440 | Homo sapiens | P01008 (AlphaFold model) |
| Antithrombin-III | L | protein | 432 | Homo sapiens | P01008 (AlphaFold model) |
>4EB1_1 Antithrombin-III (chains I) HGSPVDICTAKPRDIPMNPMCIYRSPEKKATEDEGSEQKIPEATNRRVWELSKANSRFAT TFYQHLADSKNDNDNIFLSPLSISTAFAMTKLGACNDTLQQLMEVFKFDTISEKTSDQIH FFFAKLNCRLYRKANKASKLVSANRLFGDKSLTFNETYQDISELVYGAKLQPLDFKENAE QSRAAINKWVSNKTEGRITDVIPSEAINVLVLVNTRTSTVLVLVNTIYFKGLWKSKFSPE NTRKELFYKADGESCSASMMYQEGKFRYRRVAEGTQVLELPFKGDDITMVLILPKPEKSL AKVEKELTPEVLQEWLDELEEMMLVVHMPRFRIEDGFSLKEQLQDMGLVDLFSPEKSKLP GIVAEGRDDLYVSDAFHKAFLEVNEEGSEAAASTAVVIAGRSLNPNRVTFKANRPFLVFI REVPLNTIIFMGRVANPCVK
>4EB1_2 Antithrombin-III (chains L) HGSPVDICTAKPRDIPMNPMCIYRSPEKKATEDEGSEQKIPEATNRRVWELSKANSRFAT TFYQHLADSKNDNDNIFLSPLSISTAFAMTKLGACNDTLQQLMEVFKFDTISEKTSDQIH FFFAKLNCRLYRKANKSSKLVSANRLFGDKSLTFNETYQDISELVYGAKLQPLDFKENAE QSRAAINKWVSNKTEGRITDVIPSEAINELTVLVLVNTIYFKGLWKSKFSPENTRKELFY KADGESCSASMMYQEGKFRYRRVAEGTQVLELPFKGDDITMVLILPKPEKSLAKVEKELT PEVLQEWLDELEEMMLVVHMPRFRIEDGFSLKEQLQDMGLVDLFSPEKSKLPGIVAEGRD DLYVSDAFHKAFLEVNEEGSEAAASTAVVIAGRSLNPNRVTFKANRPFLVFIREVPLNTI IFMGRVANPCVK
| ID | Name | Formula | Copies |
|---|---|---|---|
| NAG | 2-acetamido-2-deoxy-beta-D-glucopyranose | C8 H15 N O6 | 2 |
Type II antithrombin deficiency caused by a large in-frame insertion: structural, functional and pathological relevance. Martinez-Martinez, I., Johnson, D.J., Yamasaki, M. et al. J Thromb Haemost (2012) 10:1859-1866. DOI 10.1111/j.1538-7836.2012.04839.x · PubMed
Other PDB entries of the same protein (UniProt P01008 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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